Canonical Allele Identifier: CA979327002

Gene: WWOX

Linked Data

• dbSNP Id: rs2031622530
• gnomAD v4: 16-78099769-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.78099769A>G , CM000678.2:g.78099769A>G	GRCh38
NC_000016.9:g.78133666A>G , CM000678.1:g.78133666A>G	GRCh37
NC_000016.8:g.76691167A>G	NCBI36
NG_011698.1:g.5116A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000627394.3:c.-10A>G	ENSP00000485925.2:n.-10A>G
ENST00000682609.1:n.318A>G
ENST00000683286.1:n.318A>G
ENST00000683929.1:c.-10A>G	ENSP00000507689.1:n.-10A>G
ENST00000684070.1:n.320A>G
ENST00000684381.1:n.318A>G
ENST00000684452.1:n.318A>G
ENST00000684632.1:n.370A>G
ENST00000566780.6:c.-10A>G MANE Select	ENSP00000457230.1:n.-10A>G
ENST00000355860.7:c.-10A>G	ENSP00000348119.3:n.-10A>G
ENST00000402655.6:c.-10A>G	ENSP00000384238.2:n.-10A>G
ENST00000406884.6:c.-10A>G	ENSP00000384495.2:n.-10A>G
ENST00000408984.7:c.-10A>G	ENSP00000386161.3:n.-10A>G
ENST00000539474.6:c.-10A>G	ENSP00000445210.2:n.-10A>G
ENST00000561846.5:n.35A>G
ENST00000562214.5:n.114A>G
ENST00000565562.5:n.36A>G
ENST00000566662.5:c.-10A>G	ENSP00000454331.1:n.-10A>G
ENST00000566780.5:c.-10A>G	ENSP00000457230.1:n.-10A>G
ENST00000569332.5:c.-10A>G	ENSP00000454788.1:n.-10A>G
ENST00000569818.1:c.-10A>G	ENSP00000454485.1:n.-10A>G
ENST00000627394.2:c.-10A>G	ENSP00000485925.1:n.-10A>G
NM_001291997.1:c.-284A>G	NP_001278926.1:n.-284A>G
NM_016373.3:c.-10A>G	NP_057457.1:n.-10A>G
NM_130791.3:c.-10A>G	NP_570607.1:n.-10A>G
NR_120435.1:n.357A>G
NR_120436.1:n.357A>G
XM_006721195.2:c.-10A>G	XP_006721258.1:n.-10A>G
XM_011523100.1:c.-10A>G	XP_011521402.1:n.-10A>G
XM_011523101.1:c.-10A>G	XP_011521403.1:n.-10A>G
XM_011523102.1:c.-10A>G	XP_011521404.1:n.-10A>G
XM_011523103.1:c.-10A>G	XP_011521405.1:n.-10A>G
XM_011523104.1:c.-10A>G	XP_011521406.1:n.-10A>G
XM_011523105.1:c.-10A>G	XP_011521407.1:n.-10A>G
XM_011523101.3:c.-10A>G	XP_011521403.1:n.-10A>G
XM_011523103.3:c.-10A>G	XP_011521405.1:n.-10A>G
XM_011523104.3:c.-10A>G	XP_011521406.1:n.-10A>G
XM_011523105.3:c.-10A>G	XP_011521407.1:n.-10A>G
XM_017023278.2:c.-10A>G	XP_016878767.1:n.-10A>G
NM_016373.4:c.-10A>G MANE Select	NP_057457.1:n.-10A>G
NM_001291997.2:c.-284A>G	NP_001278926.1:n.-284A>G
NM_130791.4:c.-10A>G	NP_570607.1:n.-10A>G
NR_120435.2:n.116A>G
NR_120436.2:n.116A>G
NM_130791.5:c.-10A>G	NP_570607.1:n.-10A>G
NR_120436.3:n.116A>G